A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594



Internal ID15204833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86082644..86118012hg38UCSC Ensembl
Outerchr9:88697559..88732927hg19UCSC Ensembl
Outerchr9:87887379..87922747hg18UCSC Ensembl
Outerchr9:85927113..85962481hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg385626
hg195626
hg185626
hg175626
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813
SamplesNA19240
Known GenesGOLM1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6594
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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